brucellosis/edema

O link é salvo na área de transferência

Escolha o tipo de classificação

Página 1 a partir de 54 resultados

Case report: acute hydrops and spontaneous corneal perforation in a patient with keratoconus treated with colchicine for familial Mediterranean fever.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE To report a rare case of spontaneous corneal perforation after hydrops in keratoconus patients who suffer from familial Mediterranean fever and was treated systemically with Colchicine. METHODS Case report. RESULTS We report a case of a 30-year-old male with keratoconus and familial

[Chronic brucellosis with the features of meningoencephalopolyradiculoneuritis with transient edema of the brain stem].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Plantar Fasciitis and Bone Marrow Edema in Brucellosis.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

[Edemas as a form of presentation of spotted Mediterranean fever].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

A 65-year-old Italian physician affected by Familial Mediterranean fever (FMF) was hospitalized due to progressive abdominal enlargement, which had begun 6 months before admission. Physical examination revealed ascites and bilateral leg edema. Abdominal CT scan showed ascitic fluid and extensive

Coexistence of hereditary angioedema in a case of familial Mediterranean fever with partial response to colchicine.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Hereditary angioedema (HAE) is a very rare and potentially life-threatening genetic disease characterised by episodes of edema in various parts of the body, including the extremities, face, and airway. The disease is usually associated with attacks of abdominal pain. On the other hand, familial

Thrombus-in-transit entrapped in a patent foramen ovale: a complication of brucellosis.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Brucella infection may cause vascular complications such as deep venous thromboembolism. This is the first report on an entrapped thrombus in a patent foramen ovale (PFO) in a patient with Brucella infection. A 43-year-old woman was admitted with complaints of fever, dyspnea, malaise, myalgia, and

A case of brucellosis with abscess of the iliacus muscle, olecranon bursitis, and sacroiliitis.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Brucellosis is a systemic infection involving many organs and tissues. The musculoskeletal system is one of the most commonly affected. The disease can present with sacroiliitis, peripheral arthritis, spondylitis, paraspinal abscess, bursitis, and osteomyelitis. A 25-year-old male patient was

[Cutaneous polymorph manifestations of familial Mediterranean fever in a child].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

We describe the case of a 4-year-old child with Mediterranean fever characterized by cutaneous features. Familial Mediterranean fever is an autosomal recessive disorder characterized by recurrent attacks of fever and polyserositis including peritonitis, pleuritis, and arthritis. Skin involvement is

Ophthalmic manifestations in familial Mediterranean fever: a case series of 6 patients.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE To describe the ocular involvement of patients with familial Mediterranean fever (FMF) followed in a tertiary referral center. METHODS The data of 6 patients with FMF were retrospectively reviewed. Detailed ophthalmologic examinations, type of inflammation, course of the disease, number of

Superior vena cava thrombosis and obstructive sleep apnea in a patient with familial Mediterranean fever.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Familial Mediterranean fever (FMF), a paroxysmal, self-limited, inflammatory disease of unknown etiology, may result in thrombotic complications after the development of nephrotic syndrome due to amyloidosis. It has been suggested that there is increased thrombogenic activity in the blood of

Intermittent chronic neutropenia in a patient with familial Mediterranean fever.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

A 12-year-old daughter of consanguineous Moroccan parents was diagnosed with cyclic neutropenia, based on a combination of recurrent gingivostomatitis, a fluctuating neutrophil count, and several episodes of severe neutropenia. No ELA2 gene mutations were found. At age 19 years she presented with

[Nephrotic syndrome as a first manifestation of familial Mediterranean fever].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

AA amyloidosis may be a complication of Familial Mediterranean Fever (FMF). This is a case history of a female patient who did not have the classic symptoms of FMF, which usually precede the renal manifestation. The patient was admitted with edema of both legs, and the nephrotic syndrome was

Whipple's disease, familial Mediterranean fever, and adult-onset Still's disease.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Whipple's disease is a multisystem disorder thought to be caused by infection by rod-shaped bacilli. Early diagnosis remains difficult, because initial clinical features are nonspecific. Ultrasonography and computed tomographic scanning were used to demonstrate distinctive lymphadenopathy in

Familial Mediterranean fever in which Crohn's disease was suspected: a case report.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

BACKGROUND Familial Mediterranean fever is a hereditary autoinflammatory disease, mainly characterized by periodic fever and serositis. The level of awareness about familial Mediterranean fever is far from sufficient, and it is assumed that there may be many patients with this disease who are under

Junte-se à nossa
página do facebook

Herbal & Natural Medicine

O mais completo banco de dados de ervas medicinais apoiado pela ciência

Funciona em 55 idiomas
Curas herbais apoiadas pela ciência
Reconhecimento de ervas por imagem
Mapa GPS interativo - marcar ervas no local (em breve)
Leia publicações científicas relacionadas à sua pesquisa
Pesquise ervas medicinais por seus efeitos
Organize seus interesses e mantenha-se atualizado com as notícias de pesquisa, testes clínicos e patentes

Digite um sintoma ou doença e leia sobre ervas que podem ajudar, digite uma erva e veja as doenças e sintomas contra os quais ela é usada.
* Todas as informações são baseadas em pesquisas científicas publicadas